Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs713729
PICK1
1.000 0.040 22 38059462 intron variant T/A snv 0.20 2
rs7863476
PLAA
1.000 0.040 9 26915927 intron variant G/A;C snv 0.29 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs6046396
RIN2
20 19871859 non coding transcript exon variant G/A snv 0.68 2
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs6081541
SLC24A3
1.000 0.040 20 19232246 intron variant A/G snv 0.20 2
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs1959536
TRIM9
1.000 0.040 14 50980053 intron variant T/G snv 9.7E-02 2
rs737864
TXNRD2 ; COMT
1.000 0.040 22 19942636 intron variant C/T snv 0.23 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3
rs2619539
DTNBP1
0.925 0.040 6 15620624 intron variant C/A;G snv 3
rs989638
GRIA3
0.925 0.040 X 123239256 intron variant C/G;T snv 3
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 3
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3